Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue.
There is considerable interest in the development of vaccination strategies that would elicit strong tumor-specific CTL responses in cancer patients. One strategy consists of using recombinant viruses encoding amino acid sequences corresponding to natural CTL-defined peptide from tumor Ags as immuno...
मुख्य लेखकों: | , , , , , , , , , |
---|---|
स्वरूप: | Journal article |
भाषा: | English |
प्रकाशित: |
2000
|
_version_ | 1826299664341663744 |
---|---|
author | Valmori, D Lévy, F Miconnet, I Zajac, P Spagnoli, G Rimoldi, D Liénard, D Cerundolo, V Cerottini, J Romero, P |
author_facet | Valmori, D Lévy, F Miconnet, I Zajac, P Spagnoli, G Rimoldi, D Liénard, D Cerundolo, V Cerottini, J Romero, P |
author_sort | Valmori, D |
collection | OXFORD |
description | There is considerable interest in the development of vaccination strategies that would elicit strong tumor-specific CTL responses in cancer patients. One strategy consists of using recombinant viruses encoding amino acid sequences corresponding to natural CTL-defined peptide from tumor Ags as immunogens. However, studies with synthetic tumor antigenic peptides have demonstrated that introduction of single amino acid substitutions may dramatically increase their immunogenicity. In this study we have used a well-defined human melanoma tumor Ag system to test the possibility of translating the immunological potency of synthetic tumor antigenic peptide analogues into recombinant vaccinia viruses carrying constructs with the appropriate nucleotide substitutions. Our results indicate that the use of a mutated minigene construct directing the expression of a modified melanoma tumor Ag leads to improved Ag recognition and, more importantly, to enhanced immunogenicity. Thus, recombinant vaccinia viruses containing mutated minigene sequences may lead to new strategies for the induction of strong tumor-specific CTL responses in cancer patients. |
first_indexed | 2024-03-07T05:05:23Z |
format | Journal article |
id | oxford-uuid:d9bd8ce3-459f-459f-a919-3a6c60d5dfe5 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T05:05:23Z |
publishDate | 2000 |
record_format | dspace |
spelling | oxford-uuid:d9bd8ce3-459f-459f-a919-3a6c60d5dfe52022-03-27T08:58:08ZInduction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d9bd8ce3-459f-459f-a919-3a6c60d5dfe5EnglishSymplectic Elements at Oxford2000Valmori, DLévy, FMiconnet, IZajac, PSpagnoli, GRimoldi, DLiénard, DCerundolo, VCerottini, JRomero, PThere is considerable interest in the development of vaccination strategies that would elicit strong tumor-specific CTL responses in cancer patients. One strategy consists of using recombinant viruses encoding amino acid sequences corresponding to natural CTL-defined peptide from tumor Ags as immunogens. However, studies with synthetic tumor antigenic peptides have demonstrated that introduction of single amino acid substitutions may dramatically increase their immunogenicity. In this study we have used a well-defined human melanoma tumor Ag system to test the possibility of translating the immunological potency of synthetic tumor antigenic peptide analogues into recombinant vaccinia viruses carrying constructs with the appropriate nucleotide substitutions. Our results indicate that the use of a mutated minigene construct directing the expression of a modified melanoma tumor Ag leads to improved Ag recognition and, more importantly, to enhanced immunogenicity. Thus, recombinant vaccinia viruses containing mutated minigene sequences may lead to new strategies for the induction of strong tumor-specific CTL responses in cancer patients. |
spellingShingle | Valmori, D Lévy, F Miconnet, I Zajac, P Spagnoli, G Rimoldi, D Liénard, D Cerundolo, V Cerottini, J Romero, P Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue. |
title | Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue. |
title_full | Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue. |
title_fullStr | Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue. |
title_full_unstemmed | Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue. |
title_short | Induction of potent antitumor CTL responses by recombinant vaccinia encoding a melan-A peptide analogue. |
title_sort | induction of potent antitumor ctl responses by recombinant vaccinia encoding a melan a peptide analogue |
work_keys_str_mv | AT valmorid inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT levyf inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT miconneti inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT zajacp inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT spagnolig inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT rimoldid inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT lienardd inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT cerundolov inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT cerottinij inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue AT romerop inductionofpotentantitumorctlresponsesbyrecombinantvacciniaencodingamelanapeptideanalogue |